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Transcript
Herbal/Drug Interactions
Gary W. Elmer
11/12/09
Table 1. Enrollees in CHS Studya
Total enrolled: 5849
White:
4925 (84)
Black:
924 (16)
Male:
2478 (42)
Female:
3371 (58)
Study period
1
2
3
Total users
4373
4351
3919
Rx users
3994 (91)
3891 (89)
3533 (90)
CAM users
278 (6)
295 (7)
504 (13)
Vitamin/mineral 1713 (39)
1707 (39)
1678 (43)
users
OTC users
2635 (60)
2720 (63)
2263 (58)
Rx plus CAM
238 (5)
243 (6)
411 (11)
Rx, CAM, OTC 264 (6)
270 (6.2)
459 (11.7)
a
The number in parentheses is the percent of the enrolled
Elmer et al. Ann Pharmacother. 2007;40:1617-24.
4
3561
3259 (92)
533 (15)
2081 (58)
2219 (62)
463 (13)
511 (14.4)
Table 4a
Significant Risk of CAM-drug Adverse Interaction n=5052 (16,173 interviews)
Potential Event
Mechanisma
Numberb
Occurrencesc
no. patients
all occurrences
Risk of bleeds
Aspirin
Garlic23;25-27
PD
147
214
Ginkgo24;28
PD
102
127
Garlic25-27
PD
13
16
Ginkgo29
PD
7
7
Ginseng32;33
PKd
3
3
Garlic23;25-27
PD
4
6
Ginkgo24;30;31;54
PD
2
3
PD
3
3
Warfarin
Ticlopidine
Pentoxifylline
Ginkgo24;30;31
Total
281 (5.6%)
Elmer et al. Ann Pharmacother 2007;41:1617-1624
380
Table 4b
Significant Risk of CAM-drug Adverse Interaction
Potential Event
Mechanisma Numberb
Decreased drug benefit
Digoxin
St. John’s wort21;34
Felodipine
St. John’s wort21;52
Tamoxifen
Garlic41
Occurrencesc
PKe
2
2
PKf
2
2
PKf
4
5
PD
PD
3
2
3
2
Grand Total
294
393
Garlic interactions:
Ginkgo interactions:
Garlic plus ginkgo:
168
114
282 (96%)
241
140
381 (97%)
Other
Furosemide/Aloe55
Thyroid/Kelp56
Elmer et al. Ann Pharmacother 2007;41:1617-1624
Steps for Detecting and Advising on
Herbal/Drug Interactions
– Is the patient taking any herbal
supplements?
– Does the herbal have efficacy for the
intended use?
– Is the product reliable? (i.e.,what are
they REALLY taking?)
– Is the Rx drug one with a narrow
therapeutic margin?
•
•
•
•
•
•
Evaluation of Herbal/Drug Interactions
Speculative or Theoretical
– e.g. St. John’s Wort and tyramine containing
foods due to MAOI effects or evening primrose
oil and risk for bleeds with warfarin
In vitro effects
– e.g. ginkgo and microsomal studies showing
inhibition of CYP2C9
In vivo - animal studies
– e.g. kava and alcohol
In vivo - human case reports
– e.g. ginkgo and warfarin bleeds
In vivo - healthy human volunteer studies
– e.g. indinivir and St. John’s Wort
In vivo - clinical studies in patients
Important Criteria for Evaluation of a Human
Herbal/Drug Interaction Report
• Reputable standardized product used and carefully
described?
• Product used analyzed for marker compounds?
• Same batch used throughout study?
• Doses appropriate?
• Steady state study to discern CYP induction?
• Is observation consistent with known mechanisms of
action?
• Is observation consistent with literature observations?
• Randomized, placebo controlled human volunteer
study with appropriate n?
Relative Levels of P450 isozymes
in human liver
28%
30%
7%
13%
20%
2%
CYP 3A4
CYP2C
CYP2D6
CYP1A2
CYP2E1
Other
Interactions with St. John’s Wort
-cyclosporin• Study: 2 case reports
– case 1: 61yr had transplant 11mos earlier;
cyclosporin, azathioprine, steroids for 11 mos.
Unexplained heart failure noted after SJW
started.
– case 2: 63yr had transplant 20mos earlier:
same senario as case 1.
Ref: Ruschitzka et al. Lancet 355:548-549,2000
Summary of SJW Interactions
(adapted from Henderson et al. Br J Clin Pharmacol 2002;54:349-346)
Drug
HIVprotease inhibitors
CYP
Induce 3A4
Effect Management
Stop and measure

viral load
Induce 3A4

Induce 2C9


oral contraceptives
Induce Pglycoprotein
Induce 3A4
anticonvulsants
Induce 3A4

digoxin

theophylline
Induce Pglycoprotein
Induce 1A2
Triptans
(sumatriptan)
SSRI
(fluoxetine,sertraline, etc)
Increase
serotonin
Increase
serotonin

Stop and measure
viral load
Stop and adjust warfarin
dose
Stop and adjust
cyclosporine dose
Stop and use alternate
birth control
Stop and adjust
anticonvulsant dose
Stop and adjust digoxin
dose
Stop and adjust
theophylline dose
Stop

Stop
(nelfinavir,ritonavor,saquinavir)
HIVnon-nucleoside RTI
(efavirenz,nevirapine)
warfarin
cyclosporin


St. John’s Wort
• Summary
– Efficacy: good evidence for mild to
moderate depression
– Safety: don’t combine with other
medications unless under close monitoring;
possible photosensitivity
– Drug interactions: a problem! Is a broad
spectrum P450 inducer and a pglycoprotein inducer.
– Product selection: want standardized
extract containing about 0.3% hypericin or
1-2% hyperforin
– Dose: about 300mg TID for treatment
– GWE: avoid concurrent use with all but the
safest of drugs
Bleeds associated with ginkgo
use
Patient G
inkgouse
age
O
ther
therapy
Bleed
70
1week
Aspirin
Iris
1
78
2m
os
W
arfarin
Intracerebral
2
33
2years
None
Subdural
3
61
6m
os
None
Subarachnoid 4
1.
2.
3.
4.
NEJM336:1108,1997
Neurology50:1933-1934,1998
Lancet 352:36-37,1998
Neurology46:1775-1776,1996
ref
Ginkgo-warfarin interactions?
Non-linear Regression
Ki Values
Isoform
Type of Inhibition
Ki (g/ml)

CYP1A2
Mixed
11.2
0.6
Competitive
2.1
---
CYP2A6
Mixed
21.2
2.1
CYP2C9
Competitive
9.1
---
CYP2D6
Competitive
133.1
---
CYP3A4
Mixed
17.0
2.5
Mohutsky et al. Am J Ther 2006;13:24-31
Tolbutamide Human Study (CYP 2C9 probe)
-6 Subjects (3 males, 3 females)
-Subjects ingested 500mg tolbutamide and
collected 6-12 hour urine (Control phase)
-Followed by a 2 week wash-out period
-Subjects then ingested two 60mg Ginkgo biloba
extract tablets 2 times a day for 3 days
-The morning of day 4 patients received a 500mg
dose of tolbutamide along with the ginkgo and
collected 6-12 hour total urine (Ginkgo phase)
Tolbutamide dose
2 week wash-out period
Mohutsky et al. Am J Ther 2006;13:24-31
Ginkgo
biloba
dose
Tolbutamide
dose
Comparison of Tolbutamide Metabolic Ratios
Metabolic Ratio (4methylhydroxytolbutamide +
carboxytolbutamide / tolbutamide)
1400
1200
1000
800
Control
Ginkgo
680  323
610  327
600
400
200
0
Control
Mohutsky et al. Am J Ther 2006;13:24-31
Ginkgo
Diclofenac-Ginkgo Interaction (CYP 2C9 probe)
12 healthy non-smoking subjects were recruited (8
males 4 females)
50 mg diclofenac potassium (immediate release) was
administered every 12 hours for 14 days
On day 8, 120 mg of Ginkgo biloba extract was
added to the diclofenac regimen.
On days 7 and 14 plasma collected at times (0, 0.5,
1,2,4,6,8,10, and 12 hrs)
12 hour urine collected
Day 7 blood draw
Day 14 Blood draw
Diclofenac 50 mg every 12 hours
Ginkgo biloba 120 mg every 12 hours
Mohutsky et al. Am J Ther 2006;13:24-31
Comparison of Diclofenac Clearances from Plasma
1.6
1.4
Cl/F (L/hr/kg)
1.2
1
0.8
Control
Ginkgo
0.64  0.36
0.61  0.33
0.6
0.4
0.2
0
Control
Mohutsky et al. Am J Ther 2006;13:24-31
Ginkgo
Ginkgo biloba - Diclofenac Tolbutamide Human Studies
Conclusions
•
No difference was observed in the metabolic ratio
between the two arms of the study (tolbutamide
alone and tolbutamide + Ginkgo)
•
No difference was seen between the clearances of the
two arms of the study ( diclofenac alone and
diclofenac + Ginkgo)
•
Ginkgo extract does not appear to interact with
CYP2C9 substrates in humans
Jiang et al. Br J Clin Pharmacol 2005;59:425-432.
N=12 ginkgo for 7d; warfarin alone or in combination with ginkgo or
ginger
CoQ10 and Ginkgo on Warfarin
3.2
3
INR
2.8
2.6
2.4
2.2
2
CoQ10
Ginkgo
Placebo
Engelsen et al, Thromb Haemost 2002;87:1075-6. N=21, double blind, crossover. Rx=1 month with 2 week
washout. Dose of warfarin did not change.
Ginkgo and coagulation and
pharmacodynamic interactions with
antiplatelet adhesion inhibitors
Coagulation in healthy adults (in absence of other
drugs)
Kohler et al. Blood Coagul Fibrinolysis. 2004;15:303-9.
(company study).
No effect on coagulation parameters in healthy adults
after 7d of EGb761 120mg/d. n=50.
Gardner et al. Blood Coagul Fibrinolysis 2007;18:287-293
Aspirin 325mg/d for two weeks prior to 4 weeks Ginkgold 300mg/d
Bleed times; single dose n=80 cilostazol=Pletel clopidrogrel= Plavix
Gurley et al. Clin Pharmacol Ther 2002;72:276-287 n=12 (CYP 3A4)
ginkgo-Wild Oats Markets (24% flavone glycosides, 6%
ginkgolides)(analyzed)
Ushida et al. J Clin Pharmcol 2006;46:1290-8 n=12 CYP 3A4
probe is midazolam; note: use Ginkgold 120mg TID!
Ginkgo biloba summary
– Efficacy: questionable for dementia and
peripheral circulatory problems
– Safety: good; rare bleeding episodes
– Drug interactions: no effect on 3A4,2C9 or
2D6 but may induce 2C19 omeprazole
study); inhibits platelet adhesion;
possible (not necessarily probable!)
interaction with platelet drugs and
warfarin so avoid or close monitoring
needed.
– Product selection: look for EGb761
extract
– Dose: 1-2 60mg tabs, BID
– GWE: to be on the safe side, best to avoid use
with warfarin, aspirin, and platelet drugs.
Garlic summary
– Efficacy: ? benefit for use in hyperlipidemia.
Possible other cardiovascular benefits.
– Safety: good
– Drug interactions: warfarin; possibly aspirin
and other antiplatelet adhesion drugs
(pharmacodynamic interaction); not with HIV
drugs (other 3A4 substrates?) but depends on
product (pharmacokinetic interaction) (maybe
raw garlic induces 3A4 but not extracts??)
– Product selection: Suggest enteric coated
tablets standardized to about 4mg allicin
yield/tablet
– Dose: equivalent of about 4g (2-3 cloves) of
fresh garlic per day i.e. 8-12 mg allicin/d
– GWE: garlic supplements should be avoided
with warfarin (and possibly antiplatelet drugs)
and HIV drugs
Soy
– Efficacy: increased soy ingestion may
decrease hot flashes and other
postmenopausal symptoms;
cardiovascular benefits as well.
– Safety: good but use in breast cancer
may be risky
– Drug interactions: not with with
tamoxifen but effect on CYP3A4 is
unlikely
– Product selection: soy or isoflavones
– Dose: about 20-40g of soy protein has
been used. This contains 30-50mg of
isoflavones.
– GWE: not with tamoxifen but otherwise OK
Ginseng
Efficacy: some evidence for applications in
geriatric patients (improved “quality of
life”) and in diabetes
Safety: good;
Drug interactions: no apparent induction of
CYP 3A4 but induction of 2C9 (warfarin)
with Am ginseng (Panax quinquifolius) but
maybe not Panax ginseng. May precipitate
hypoglycemia with insulin or oral
hypoglycermics.
Product selection: product should be
standardized so dose is 4-7%
ginsenosides/d
GWE: safest to avoid use with warfarin and
hypoglycemics
Echinacea
• Summary
Efficacy: evidence for treatment not prevention
Safety: good; rare allergy
Drug interactions: Pharmacodynamic: don’t give to
patients taking immunosuppressive drugs
Pharmacokinetic: may inhibit 1A2; may inhibit intestinal
3A4 but induce hepatic so clinical significance
unclear; effect on 2C9 is considered minor
Product selection: want standardized extract containing
about 4% phenolics. (GWE recommends Echinamide
in 2008)
Dose: about 250mg QID for treatment
GWE: echinacea/drug interactions are only of minor
concern
Herbs with clotting problems reported in humans
Ginkgo and garlic and St. John’s wort- see earlier notes
Evening primrose oil -
human study showed 40% increase in bleed time but no other
reports
Borage seed oil -
same as evening primrose oil
Vitamin E -
doses >1200 i.u./d can increase bleed time
Cranberry juice
case reports of increased INR (salicylic acid? CYP 2C9 inhibition?)
but in vivo study showed no change in flurbiprofen (CYP 2C9
substrate) in vivo
Lycium barbarum
case report of increased INR
Danshen -
case reports of increased INR with warfarin
Dong quai -
case reports of increased INR with warfarin
American Ginseng -
decreased INR with warfarin (Panax quinquifolius)
Green tea -
case report of decreased INR with warfarin but huge amount
CoQ10 -
case reports of decreased INR with warfarin but human study
showed no effect on INR
Glucosamine-
increased INR cases with warfarin
Chondroitin-
increased INR cases with warfarin
Fig. 1 Patient INR Values
Tea Taken
5
7/27
INR value
4
3
1/12/00
2/16
12/15/99
11/10
2
6/30
4/5
8/29 9/7
8/2
8/7
5/26
10/8
8/18
11/7
1
0
10/17/99
12/6
1/25 /00
3/15
5/4
Date
6/23
8/12
10/1
From: Lam AY, Mohutsky MA and Elmer GW. Probable herbal/drug interaction between
warfarin and a common Chinese herb, Lycium barbarum. Ann Pharmacother 2001;35:11991201
11/20
Gary Elmer’s assessment of herbal/drug interaction potential (in rank order
of significance)(11/13/09)
1.
St. John’s wort – induces CYP and Pgp; don’t take with other drugs unless the
drugs have a large therapeutic range and are not “life saving” drugs
2.
American ginseng (Panax quinquefolius) – induces CYP2C9; not with warfarin,
tolbutamide and other 2C9 substrates;
3.
Goldenseal – induces CYP3A4 and 2D6. This herbal is not recommended due to
lack of efficacy proof and potential interactions
4.
Garlic and ginkgo – don’t take with antiplatelet adhesion drugs or aspirin or with
warfarin (risk of bleeds); this is a pharmacodynamic effect. Risk may be over
stated based on recent evidence.
5.
Ginkgo may induce CYP2C19 so may lower 2C19 substrates like omeprazole,
phenytoin and diazepam
6.
Echinacea may induce CYP1A2 so may lower 1A2 substrates like caffeine,
theophylline and acetaminophen
Seem to have low
pharmacokinetic drug interaction
potential based on recent studies
•
•
•
•
•
•
Ginger
Valerian
Milk thistle
Saw palmetto
Black cohosh
CoQ10
References with Good Herbal/Drug
Interactions Discussion
–“Top 100 Drug Interactions” Hansten
PD and Horn JD. H&H Publications 2008
–Natural Medicines Comprehensive
Database.
Online version updated “daily”. UW Healthlinks
http://www.naturaldatabase.com/; $92
Recent Reviews
•Izzo AA and Ernst E. Interactions between herbal
medicines and prescribed drugs: an updated systematic
review. Drugs. 2009;69(13):1777-98
•Skalli S, Zaid A, Soulaymani R. Drug interactions with
herbal medicines. Ther Drug Monit. 2007
Dec;29(6):679-86
•Chavez ML, Jordan MA, Chavez PI. Evidence-based
drug--herbal interactions.Life Sci. 2006;78:2146-57.
What can we do?
• dialog with NDs and other prescribers
• recommend the best products
• ask patients about herbals they may be taking
• herbals should not usually be recommended for
acute or serious illnesses
• avoid herbal use with drugs with narrow
therapeutic window, esp. warfarin, cyclosporin,
digoxin, HIV protease inhibitors, theophylline,
carbamazepine
• stay informed